In the ﬁrst stage of the base excision repair pathway the enzyme uracil DNA glycosylase (UNG) recognizes and excises uracil (U) from DNA ﬁlaments. U repair is believed to occur via a multistep base-ﬂipping process, through which the damaged U base is initially detected and then engulfed into the enzyme active site, where it is cleaved. The subtle recognition mechanism by which UNG discriminates between U and the other similar pyrimidine nucleobases is still a matter of active debate. Detailed structural information on the diﬀerent steps of the base-ﬂipping pathway may provide insights on it. However, to date only two intermediates have been trapped crystallographically thanks to chemical modiﬁcations of the target and/or of its complementary base. Here, we performed force-ﬁeld based molecular dynamics (MD) simulations to explore the structural and dynamical properties of distinct UNG/dsDNA adducts, containing A:U, A:T, G:U, or G:C base pairs, at diﬀerent stages of the base-ﬂipping pathway. Our simulations reveal that if U is present in the DNA sequence a shortlived extra-helical (EH) intermediate exists. This is stabilized by a water-mediated H-bond network, which connects U with His148, a residue pointed out by mutational studies to play a key role for U recognition and catalysis. Moreover, in this EH intermediate, UNG induces a remarkable overall axis bend to DNA. We believe this aspect may facilitate the ﬂipping of U, with respect to other similar nucleobases, in the latter part of the base-extrusion process. In fact, a large DNA bend has been demonstrated to be associated with a lowering of the free energy barrier for base-ﬂipping. A detailed comparison of our results with partially ﬂipped intermediates identiﬁed crystallographically or computationally for other base-ﬂipping enzymes allows us to validate our results and to formulate hypothesis on the recognition mechanism of UNG. Our study provides a ﬁrst ground for a detailed understanding of the UNG repair pathway, which is necessary to devise new pharmaceutical strategies for targeting DNA-related pathologies.
Structural Role of Uracil DNA Glycosylase for the Recognition of Uracil in DNA Duplexes. Clues from Atomistic Simulations / Franco, D.; Sgrignani, J.; Bussi, G.; Magistrato, A.. - In: JOURNAL OF CHEMICAL INFORMATION AND MODELING. - ISSN 1549-9596. - 53:6(2013), pp. 1371-1387.
|Titolo:||Structural Role of Uracil DNA Glycosylase for the Recognition of Uracil in DNA Duplexes. Clues from Atomistic Simulations|
|Autori:||Franco, D.; Sgrignani, J.; Bussi, G.; Magistrato, A.|
|Data di pubblicazione:||2013|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1021/ci4001647|
|Appare nelle tipologie:||1.1 Journal article|